Fluorine-containing polymers and preparation and use thereof

ABSTRACT

Group IV organometallic compounds, e.g. alkylsilane, or alkylsiloxane compounds, are used as chain tranfer agent in the radical initiated polymerization of ethylenically unsaturated monomers, to give polymers comprising non-ionic end groups.

This is a division of application Ser. No. 07/869,943 filed Apr. 17,1992 now U.S. Pat. No. 5,208,305.

This invention relates to fluorine-containing polymers and theirpreparation and use. In another aspect, this invention relates tomethods of free-radical polymerization of ethylenically unsaturatedmonomers in the presence of chain-transfer agents, and to the resultingpolymers and shaped articles thereof.

Fluorine-containing polymers, or fluoropolymers, with a carbon-carbonbackbone chain are an important class of polymers and include forexample, fluoroelastomers and fluoroplastics. Within this class arepolymers of high thermal-stability and concurrent usefulness at hightemperatures, and extreme toughness and flexibility at very lowtemperatures. Many of these polymers are almost totally insoluble in awide variety of organic solvents, and are chemically inert. Some haveextremely low dielectric loss and high dielectric-strength, and mosthave unique nonadhesive and low-friction properties. F. W. Billmeyer,Textbook of Polymer Science, 3rd ed., pp 398-403, John Wiley & Sons, NewYork (1984).

Fluoroelastomers, particularly the copolymers of vinylidene fluoridewith other ethylenically unsaturated halogenated monomers, such ashexafluoropropene, have particular utility in high temperatureapplications, such as seals, gaskets, and linings--see, for example,Brullo, R. A., "Fluoroelastomer Rubber for Automotive Applications,"Automotive Elastomer & Design, June 1985, "Fluoroelastomer Seal UpAutomotive Future," Materials Engineering, October 1988, and"Fluorinated Elastomers," Kirk-Othmer, Encyclopedia of ChemicalTechnology, Vol. 8, pp. 500-515 (3rd ed., John Wiley & Sons, 1979).

Fluoroplastics, particularly polychlorotrifluoroethylene,polytetrafluoroethylene, copolymers of tetrafluoroethylene andhexafluoropropylene, and poly(vinylidene fluoride), have numerouselectrical, mechanical, and chemical applications. Fluoroplastics areuseful, for example, in wire, electrical components, seals, solid andlined pipes, and pyroelectric detectors. Polychlorotrifluoroethylene iscompatible with liquid oxygen, and remains tough at cryogenictemperatures. See, for example, "Organic Fluorine Compounds,"Kirk-Othmer, Encyclopedia of Chemical Technology, vol. 11, pp. 20, 21,32, 33, 40, 41, 48, 50, 52, 62, 70. 71. John Wiley & Sons, (1980).

Fluorine-containing polymers can be prepared by free-radical initiatedpolymerization of one or more fluorine-containing ethylenicallyunsaturated monomers. Free radicals are typically formed by thedecomposition of a free-radical initiator. Free-radical initiators maybe decomposed by light, heat, high energy radiation, or as a result ofoxidation-reduction reactions. When free radicals are generated in thepresence of free-radical polymerizable ethylenically unsaturatedmonomers a chain reaction occurs producing polymer. The polymer can beprepared by polymerization of monomers in bulk, in solution, inemulsion, or in suspension. Fluoroelastomers and fiuoroplastics arepreferably prepared by aqueous emulsion or suspension polymerizationbecause of the rapid and nearly complete conversion of monomers, easyremoval of the heat of polymerization and ready isolation of thepolymer. Emulsion or suspension polymerization typically involvespolymerizing monomers in an aqueous medium in the presence of aninorganic free-radical initiator system, and surfactant or suspendingagent.

Polymers of low molecular-weight can be prepared by polymerizingmonomers in the presence of a chain-transfer agent. Chain-transferagents react with the growing polymer-chain. In this reaction, thegrowing polymer-chain is terminated and the chain-transfer agent isconverted into a radical. This newly-formed free-radical typically canimmediately react with monomer, thereby initiating the polymerization ofa new polymer-chain. Examples of conventional chain-transfer agents arecarbon tetrachloride, acetone, diethyl malonate, and dodecylmercaptan.Chain-transfer activity varies greatly with changes in solvents andmonomers.

The chain-transfer constants of triphenylsilane and triethyisilane inthe thermal polymerization of styrene were measured in J. Curtice, H.Gilman, and G. Hammond, "A Study of Organosilicone Free Radicals," J.Am. Chem. Soc., Vol. 79, pp. 4754-4759, (1957).

In aqueous emulsion or suspension polymerization of fluorine-containingethylenically unsaturated monomer, conventional chain-transfer agentsgenerally can terminate a growing polymer-chain but generally do notimmediately react with monomer to initiate a new polymerization. As aresult, the polymerization generally is slow and most polymer chainscontain an ionic end-group due to initiation by ionic radical-initiator,e.g., sulfate radical ion.

Ionic or polar end-groups generally are not desirable because ofdetrimental effects on rheology. U.S. Pat. No. 4,524,197 (Khan) statesthat the presence of acid end-groups detrimentally effects theprocessing characteristics of fluoroelastomers since these groupsincrease the viscosity of the polymer and interfere with curing systems,especially those based on quaternary phosphonium salts.

Ionic or polar end-groups may also reduce the thermal stability ofcertain fluorine-containing polymers. U.S. Pat. No. 4,743,658 (Imbalzanoet al.) states that perfluorinated resins with certain end groups,especially --COF, --CONH₂, and --CF₂ CH₂ OH, can be chemically reactiveand thermally unstable. Such end groups evolve HF, which is generated bythe oxidation, hydrolysis and/or thermal decomposition of these endgroups.

Polymers with non-ionic end groups can be prepared by the use ofnon-ionic free-radical initiators, e.g., azo-bisisobutyronitrile orbenzoyl peroxide. However, most non-ionic free-radical initiators areinsoluble in water and are therefore not suitable for aqueous emulsionor suspension polymerization of fluorine-containing monomers. Theemployment of water-insoluble initiators would require the use oforganic co-solvents and/or seed latices produced with water-solubleinitiators.

Briefly, in one aspect, the present invention provides a method for thepreparation of fluorine-containing polymer comprising polymerizing,under free-radical conditions, a polymerizable mixture comprisingfluorine-containing ethylenically unsaturated monomer, e.g., CF₂ ═CF₂,and a non-free-radically polymerizable organometallic compoundcomprising a group IV metal atom, e.g., Si, and an aliphatic carbon atombonded directly to said metal atom and to a hydrogen atom, e.g.,tetraalkylsilane, tetraalkyistannane, or tetraalkylgermane.

In another aspect, this invention provides a fluorine-containing polymercomprising a fluorine-containing, saturated, carbon-carbon backbonechain comprising interpolymerized units derived from fluorine-containingethylenically unsaturated monomer, and an organometallic group, derivedfrom a non-free-radically polymerizable organometallic compound,comprising a group IV metal atom and an aliphatic carbon atom bondeddirectly to said metal atom.

The polymerization method of this invention can be used in aqueousemulsion or suspension polymerization to rapidly prepare lowmolecular-weight fluorine-containing polymers that are easy to process.These results can be obtained with low levels of free-radical initiatorand organometallic compound (conventional aqueous emulsion or suspensionpolymerization of fluorine-containing monomer typically uses largeamounts of both free-radical initiator and chain-transfer agent in orderto obtain low molecular-weight and rapid polymerization).

Suitable monomcrs for use in the method and polymer of this inventioninclude the terminally unsaturated monoolefins typically used for thepreparation of fluorine-containing polymers such as vinylidene fluoride,hexafluoropropene, chlorotrifluoroethylene, 2-chloropentafluoropropene,perfluoroalkyl vinyl ethers, e.g., CF₃ OCF═CF₂ or CF₃ CF₂ OCF═CF₂,tetrafluoroethylene, 1-hydropentafluoropropene,2-hydropentafluoropropene, dichlorodifluoroethylene, trifluoroethylene,1-dichlorofluoroethylene, vinyl fluoride, and mixtures thereof.Perfluoro-1,3-dioxoles such as ##STR1## may also be used. Theperfluoro-1,3-dioxole monomers and their copolymers are described, forexample, in U.S. Pat. No. 4,558,141 (Squire). Certainfluorine-containing di-olefins are also useful, such as,perfluorodiallylether and perfluoro-1,3-butadiene. Saidfluorine-containing monomer, or fluoromonomer, may also be copolymerizedwith fluorine-free terminally unsaturated monoolefin comonomers, e.g.,ethylene or propylene. Preferably at least 5% by weight of all monomersin said polymerizable mixture are fluorine-containing. Saidfluorine-containing monomer may also be copolymerized with iodine- orbromine-containing cure-site comonomers in order to prepare peroxidecurable polymers, e.g., fluoroelastomers. Suitable cure-site monomersinclude terminally unsaturated monoolefins of 2 to 4 carbon atoms suchas bromodifluoroethylene, bromotrifluoroethylene, iodotrifluoroethylene,and 4-bromo-3,3,4,4-tetrafluorobutene-1. Preferably, all or essentiallyall of the comonomers in said polymerizable mixture are ethylenicallyunsaturated monomers.

Preferred group IV metals in the organometallic compounds useful in thisinvention are silicon, germanium, and tin. Preferred organometalliccompounds are relatively low molecular weight compounds comprising from1 to 10 group IV metal atoms, or oligomeric liquids, oils, or greases,e.g. silicone oils, comprising from 10 to 200 group IV metal atoms. Saidmetal atoms are bonded directly to each other, or linked to each otherthrough carbon atoms or hetero atoms, e.g., O, N, S, P and the like,e.g., (CH₃)₃ Si--NH--Si(CH₃)₃. Silanes, silazanes, and siloxanes areparticularly preferred.

A class of organometailic compounds useful in this invention can berepresented by the formula

    R--[(R).sub.2 M]z--[(Q).sub.x --M(R).sub.2 ].sub.y --CH(R).sub.2 I

where M is Si, Sn, or Ge, Q is a divalent linking group, e.g. --S--,--O--, alkylene, e.g., --CH₂ --, --NR--, arylene, e.g., C₆ H₄ (i.e.,phenylene), or combinations thereof, each R is independently H, alkyl,aryl, or combinations thereof such as alkaryl or aralkyl, x is 0 or 1, zis 0 or 1, y is an integer from 1 to 9. As used herein, alkyl andalkylene includes substituted and cyclic moieties, e.g., fluoroalkyl,and cycloalkyl.

Representative examples of such compounds are ##STR2##

A second class of organometallic compounds useful in this invention isthe class of cyclic compounds where the metal atoms are part of a ring.Representative examples of such compounds are cyclic silanes andsiloxanes such as: ##STR3##

The method of this invention can comprise the use of certain group IVorganometallic compounds in otherwise conventional free-radicalpolymerization of ethylenically unsaturated monomers. Such conventionalpolymerization includes free-radical polymerization of the monomersalone or as solutions, emulsions, or dispersions in an organic solventor water. Polymerization in an aqueous emulsion or suspension is oftenpreferred because of the rapid and nearly complete conversion ofmonomers, easy removal of the heat of polymerization and ready isolationof the polymer. Emulsion or suspension polymerization offluorine-containing monomer typically involves polymerizing monomers inan aqueous medium in the presence of an inorganic free-radical initiatorsystem, and surfactant or suspending agent.

The formation of group IV organometallic alkyl radicals is described inP. Krusic, and J. Kochi, "Electron Spin Resonance of Group IVOrganometallic Alkyl Radicals in Solution," J. Am. Chem. Soc., Vol.91,pp. 6161-6164, (1969). Alkyl derivatives of silicon, germanium, and tinwere used to generate carbon-centered radicals by removal of a hydrogenatom from a carbon atom bonded directly to the metal.

The organometailic compounds useful in the method of this invention arenon-free-radically polymerizable compounds that do not react with wateror monomer, but do react with radicals, e.g., the radical end of agrowing polymer-chain. The organometallic compound thus acts as achain-transfer agent by terminating the polymerization of onepolymer-chain and initiating the polymerization of a new polymer-chain.

Conventional inorganic free-radical initiators can be used in thefree-radical polymerization method of this invention. Emulsion andsuspension polymerization is preferred. Water-soluble inorganicperoxides known to the prior art, such as sodium, potassium, or ammoniumparsulfates, perphosphates, perborates, percarbonates, or permanganatesare useful. The free-radical initiators can be further activated byreducing agents such as sodium, potassium, or ammonium sulfite,bisulfite, metabisulfite, hyposulfite, thiosulfite, phosphite, sodium orpotassium formaldehyde sulfoxylate or hypophosphite, or by easilyoxidized metal compounds such as ferrous, cuprous, and silver salts.

Aqueous emulsion and suspension polymerizations may be carried out underconventional steady-state conditions in which, for example, themonomers, water, surfactants, buffers and catalysts are fed continuouslyto a stirred reactor under optimum pressure and temperature conditionswhile the resulting emulsion or suspension is removed continuously. Analternative technique is batch or semibatch polymerization by feedingthe ingredients into a stirred reactor and allowing them to react at aset temperature for a specified length of time or by chargingingredients into the reactor and feeding the monomer into the reactor tomaintain a constant pressure until a desired amount of polymer isformed.

The amount of organometallic compound used can vary, depending forexample on the molecular weight of polymer desired. Preferably from 0.4to 400 mmoles, and most preferably from 0.4 to 100 mmoles, oforganometallic compound are used per Kg of monomer.

The polymer of this invention comprises a fluorine-containing,saturated, carbon-carbon backbone chain whose interpolymerized units arederived from ethylenically unsaturated monomers. For example, wherevinylidene fluoride and hexafluoropropene are copolymerized theinterpolymerized units are --CH₂ --CF₂ and --CF(CF₃)--CF₂ --. Saidpolymer also comprises at least one organometallic group, derived from anon-free-radically polymerizable organometallic compound, comprising agroup IV metal atom and an aliphatic carbon atom bonded directly to saidmetal. Particularly preferred organometailic groups are silyl, silazyl,or siloxyl. Preferably, said organometallic group terminates a polymerchain or branch as an end-group.

A class of the polymers of this invention comprise an organometallicgroup (covalently bonded to the polymer) which can be represented by theformula

    R--[(R).sub.2 M].sub.z --[(Q).sub.z --M(R).sub.2 ].sub.y --

where M, Q, R, x, z, and y are as described above for formula I.

The polymers of this invention, such as fluoroelastomer gums, may becompounded and cured using conventional methods. Such polymers are oftencured by nucleophiles such as diamines, polyhydroxy compounds, orfluoroaliphatic sulfonamides. Certain polymers may be cured withperoxides. For example, the fluoroelastomers of this invention may becrosslinked with aromatic polyhydroxy compounds, such as bisphenols,which are compounded with the polymer along with a curing accelerator,such as a quaternary phosphonium salt, and acid acceptors, such asmagnesium oxide and calcium hydroxide. Particularly useful polyhydroxycompounds include 4,4'-thiodiphenol,isopropylidene-bis(4-hydroxybenzene), andhexafluoroisopropylidene-bis(4-hydroxybenzene) ("bisphenol AF") whichare described, for example, in U.S. Pat. No. 4,233,421 (Worm). Suchcrosslinking methods are described, for example, in U.S. Pat. No.4,287,320 (Kolb), 4,882,390 (Grootaert et al.), and U.S. Pat. No.5,086,123 (Guenthner et al.). A cure-site monomer susceptile tofree-radical attack is required to render polymers peroxide curable. Forexample, polymers which contain interpolymerized units derived fromiodine- or bromine-containing monomers are often peroxide-curable. Suchcure-site monomers are described, for example, in U.S. Pat. No.4,035,565 (Apotheker et al.) and U.S. Pat. No. 4,450,263 (West).

The polymers of this invention can also be compounded with processingagents, such as those conventionally used to aid in the molding orextrusion of the formulation, e.g. carnauba wax or dichlorodiphenylsulfone. Fluoroaliphatic sulfonamides can also be used as processingaids, including those of the formula R_(f) SO₂ NHR", where R_(f) is afluoroaliphatic radical such as a perfluoroalkyl, e.g., C_(n) F_(2n+1)where n is 4 to 20, or perfluorocycloalkyl, e.g,, C_(n) F_(2n-1) where nis 5 to 20, such compounds being described, for example, in AustralianPat. No. 58,641 (Guenthner et al.). Another type of processing aid whichcan be used in this invention is diorgano sulfur oxides, such as thosedescribed in U.S. Pat. No. 4,287,320 (Kolb).

Fillers can be mixed with the polymers of this invention to improvemolding characteristics and other properties. When a filler is employed,it can be added to the vulcanization recipe in amounts of up to about100 parts per hundred parts by weight of gum, preferably between about15 to 50 parts per hundred parts by weight of the gum. Examples offillers which may be used are thermal-grade carbon blacks or fillers ofrelatively low reinforcement characteristics such as clays and barytes.

The organometallic compounds useful in this invention result in polymerswhich can have a variety of non-polar, non-ionic end-groups comprising agroup IV metal atom. These non-ionic end-groups generally resuit inimproved properties such as improved thermal stability and improvedrheological behavior. Polymers with non-ionic end-groups exhibit lowerapparent viscosities during processing, e.g. injection molding, whencompared at the same shear rates to polymers with ionic end-groups. Theresulting polymers may be elastomers or plastics. The polymers may beshaped to form useful articles including O-rings, fuel-line hoses, shaftseals, and wire insulation.

The polymers of this invention can be mixed with other polymers, forexample, with polymers of higher or lower molecular weight to give abimodal molecular-weight mixture. For example, low molecular-weightpolymers of this invention can be mixed with conventionalfluorine-containing polymers to improve the processing characteristicsthereof.

EXAMPLES

In the following Examples and Comparative Examples polymers wereprepared. Viscosity of the resulting polymer was determined using thefollowing test methods.

Mooney Viscosity

Mooney viscosities were measured at 121° C. using a Monsanto MooneyViscometer model MV 2000, a large rotor, 1 minute preheat, andmeasurement after 10 minutes ("ML 1+10 ©121° C."), according to ASTMD1646-81.

Inherent Viscosity

Inherent viscosity ("iv") was measured using dilute solutions of thepolymers in 2-butanone at 35° C. Three samples were run for each polymer(1.0, 0.5, and 0.25 wt. % solids). An Ostwald viscometer was used andthe iv was calculated using the following formula: iv=[ln(t/ts)]/c,where t is the time for the solution to flow between the markers, ts isthe time to flow between the markers for solvent without polymer, and cis the concentration of the solution in g/dL.

In the following Examples 1-8 and Comparative Examples C1-C4,fluoroelastomer polymers were prepared by free-radical initiatedemulsion-polymerization. The monomers utilized were vinylidene fluoride("VF₂ "), hexafluoropropene ("HFP"), and tetrafluoroethylene ("TFE").The polymers produced were either copolymers of VF₂ and HFP, orterpolymers of VF₂, HFP, and TFE.

The Examples of this invention utilized silanes and siloxanes as theorganometallic compound. The polymers of the Examples of this inventionwere analyzed by proton NMR and shown to contain at least one silane orsiloxane group.

In the Comparative Examples, diethylmalonate was used as achain-transfer agent, or no chain-transfer agent was used, instead of asilane or siloxane.

EXAMPLE 1

A solution of 9 g of K₂ HPO₄ and 3 g of K₂ S₂ O₈ in 2800 g of water wasplaced in a 4-liter pressure reactor. The reactor was evacuated andfilled with nitrogen four consecutive times and 1.8 g ofhexamethyldisilane ("HMDS") was added via syringe through a septum on ainlet valve. The contents of the reactor were stirred with a mechanicalstirrer, heated to 71° C., and the reactor was pressurized to 1.24 to1.31 MPa with a monomer mixture of 61.7 wt. % VF₂ and 38.3 wt. % of HFP.Pressure was maintained between 1.24 and 1.31 Mpa during polymerizationby adding more of the monomer mixture. After 750 g of monomer mixturehad been added, the reaction mixture was cooled to room temperature, andexcess unreacted monomer mixture was vented. The reaction time("R-Time") was 6.5 hrs. The resulting latex was coagulated by drippingit into an agitated solution of 20 grams of magnesium chloridehexahydrate in 800 mL of deionized water. The resulting copolymer of HFPand VF₂ was then washed four times with 2.5 L of hot (75° to 80° C.)deionized water, and the washed polymer gum dried overnight in acirculating air oven at 90° to 100° C.

EXAMPLES 2-4 AND COMPARATIVE EXAMPLES C1-C3

In Examples 2-4 and Comparative Examples C1-C3copolymers of HFP and VF₂were prepared as in Example 1 except with the amounts of ingredients asshown in Table 1. Example 4 and Comparative Example C3 also contained0.6 g and 2.4 g, respectively, of FC-128 fluorochemical emulsifieravailable from 3M Company. The organometallic compound used in Examples2-4 was either hexamethyldisilane (HMDS), tetramethylsilane ("TMS"), orhexamethyldisiloxane ("HMDSO"). The Comparative Examples C1-C3do notcontain organometallic compound. Comparative Examples C2 and C3 useddiethylmalonate (DEM) as chain-transfer agent. Each Example andComparative Example utilized 2800 g of deionized water and a monomermixture of 61.7 wt. % VF₂ and 38.3 wt. % HFP.

                  TABLE 1                                                         ______________________________________                                        Examples             Comparative Examples                                     2           3         4      C1    C2    C3                                   ______________________________________                                        K.sub.2 HPO.sub.4                                                                    9        9         9    9     9     6.3                                (g)                                                                           K.sub.2 S.sub.2 O.sub.8                                                              5        3         5    3     3     15.3                               (g)                                                                           chain  HMDS,    HMDSO,    TMS  none, DEM,  DEM,                               transfer                                                                             3        2         1.8  0     2     11.4                               agent, g                                                                      monomer                                                                              780      800       680  780   800   1000                               (g)                                                                           R-Time 6.5      6         4    2.5   4.5   6.5                                (hrs)                                                                         ______________________________________                                    

The polymers of the above Examples and Comparative Examples wereanalyzed for the presence of silane or siloxane groups by proton NMR.The Mooney (ML 1+10 ©121° C.) viscosity ("Mooney") was measured for eachpolymer. Where the Mooney viscosity was 0, the inherent viscosity wasalso measured. The results are summarized in Table 2.

                                      TABLE 2                                     __________________________________________________________________________                                    Comparative                                                Examples           Examples                                                   1    2    3     4  C1  C2  C3                                    __________________________________________________________________________    chain transfer agent, moles                                                                HMDS HMDS HMDSO TMS                                                                              None                                                                              DEM DEM                                                .012 .021 .012  0.20                                                                             0   .012                                                                              .071                                  Mooney       24   0    57    39 194 105 0                                     iv           --   0.15 --    -- --  --  0.18                                  __________________________________________________________________________

The proton NMR of the polymers of Examples 1-4 showed the presence ofCH₃ --Si in each polymer at 0.1 to 0.5 ppm in the spectra. The highereffectiveness of the silane and siloxane compounds as chain-transferagents for reducing molecular weight is shown in Table 2 by lowerMooney-viscosity or a lower iv which indicates lower molecular weightFor example, although Example 3 and Comparative Example C2 usedequimolar amounts of chain-transfer agent and persulfate initiator, thepolymer prepared in Example 3 had a much lower Mooney viscosity.Comparing Example 2 to Comparative Example C3 shows that lower iv wasobtained in the same reaction time but with much less persulfateinitiator and much less chain-transfer agent, when the method of thisinvention was used.

EXAMPLE 5

In Example 5 a terpolymer of HFP, VF₂, and TFE was prepared as inExample 1 except the polymerization was run in a 86-Liter reactor using45 Kg deionized water, 145 g K₂ HPO₄, 50 g HMDS, the pressure was heldconstant at 0.90 MPa instead of 1.24 to 1.31 Mpa, 18.25 Kg of a monomermixture containing 23.6 wt. % TFE, 31.5 wt. % HFP, and 44.9 wt. % VF₂was consumed, and 11.6 g FC-128 emulsifier was used. Instead of K₂ S₂O₈, 60 g of (NH₄)₂ S₂ O₈ was used as free-radical initiator. Thereaction time was 6 hrs, and the Mooney viscosity was 8.

EXAMPLES 6-7 AND COMPARATIVE EXAMPLES C3-C4

In Examples 6-7 and Comparative Examples C3-C4, terpolymers of HFP, VF₂,and TFE were prepared as in Example 5 except using the amounts ofingredients shown in Table 3. Each Example and Comparative Example used45 Kg of deionized water and the same monomer mixture as in Example 5.The reaction time for each Example and Comparative Example was 6 hours.

                  TABLE 3                                                         ______________________________________                                                                Comparative                                                  Examples         Examples                                                     5      6        7        C3     C4                                     ______________________________________                                        K.sub.2 HPO.sub.4 (g)                                                                  145      145      145    145    185                                  (NH.sub.4).sub.2 S.sub.2 O.sub.8                                                       60       40.4     40.4   60     0                                    (g)                                                                           K.sub.2 S.sub.2 O.sub.8 (g)                                                            0        0        0      0      250                                  chain-transfer                                                                         HMDS     HMDS     HMDS   DEM    DEM                                  agent (g)                                                                              50       50       9.3    54.6   185                                  FC-128 (g)                                                                             11.6     11.6     11.6   11.6   9.9                                  Mooney   8        40       145    63     2                                    ______________________________________                                    

The data in Table 3 show that high level of both persulfate andchain-transfer agent were needed to make a low-viscosity gum at areasonable reaction rate using conventional systems. For example,comparing Example 5 with Comparative Example C3 shows that when usingequal molar amounts of chain-transfer agent and initiator, the method ofthis invention resulted in a polymer with lower Mooney-viscosity.Comparative Example C4 illustrates the high levels of initiator andchain-transfer agent needed to prepare a low Mooney-viscosity polymerusing conventional methods.

EXAMPLE 8

In Example 8 a terpolymer of HFP, VF₂, and TFE was prepared as inExample 1 except using an 86-L reactor and with 45 Kg deionized water,160 g ammonium persulfate, 145 g K₂ HPO₄, 11.6 g FC-128 emulsifier, 200g HMDS, and 11.25 Kg of a monomer mixture containing 44.9 wt. % VF₂,31.5 wt. % HFP, and 23.6 wt. % TFE. The pressure was maintained duringthe run at 0.90 MPa. The temperature was 71° C. Agitation was 140 rpm,and the reaction time was 6 hrs. The Mooney viscosity was 0. Theinherent viscosity of the resulting terpolymer of HFP, VF₂, and TFE was0.10.

EXAMPLE 9

In this Example, chlorotrifluoroethylene ("CTFE") was polymerized bysuspension polymerization to form a fluoroplastic. The initiation systemconsisted of a redox initiator rather than a thermal initiator.

A 4-liter reactor was charged wilh deionized water (2600 g), K₂ HPO₄(4.0 g), Na₂ HPO₄ (4.0 g), K₂ S₂ O₈ (15 g), CuSO₄,5H₂ O (0.08 g),hexamethyl disilane (2.0 g) and CTFE (195 g). The pressure in thereactor was 0.37 MPa at 12° C. The reactor contents were agitated (350rpm) and a solution of K₂ SO₃ (10 wl. % in deionized water) was fed intothe reactor by the use of a metering pump. When a pressure drop occurred(indicative of polymerization) CTFE was fed into the reactor in order tomaintain a constant pressure of 0.37 to 0.39 MPa. Over a period of 5hours, a total of 945 g of CTFE monomer (including the 195 g precharged)was added and a total of 429 g of the 10% K₂ SO₃ solution was pumpedinto the reactor. The reactor was drained and the CTFE polymer wasisolated by filtration, washed with a mixture of a deionized water andmethanol, and the washed polymer was dried in a circulating air oven at110° C. The polymer was a white powder. A proton NMR spectrum of thepolymer revealed the presence of Si--CH₃ at 0.05 ppm.

EXAMPLES 10-21

In Examples 10-21, terpolymers of VF₂, HFP, and TFE were preparedaccording to the procedure and using reactants described in Example 5,except using 25 g (instead of 50 g) of HMDS, 40 g (instead of 60 g) of(NH₄)₂ S₂ O₈, and 11.5 g of FC-128 emulsifier. The amounts of eachmonomer are shown in Table 4. The reaction time varied from 4 to 9.5hours. The Mooney viscosity and weight percent fluorine (determined byF-NMR analysis) of each of the polymer products was determined. Theresults are shown in Table 4.

                  TABLE 4                                                         ______________________________________                                        Ex.    Monomers (wt. %) Mooney                                                No.    VF.sub.2 HFP     TFE   viscosity                                                                            Wt. % F                                  ______________________________________                                        10     40       30      30    68     69.5                                     11     40       40      20    65     69.3                                     12     50       20      30    57     67.5                                     13     50       30      20    57     67.5                                     14     60       20      20    69     65.9                                     15     60       30      10    39     65.8                                     16     30       40      30    22     71.4                                     17     70       10      20    28     64.3                                     18     30       50      20    48     71.0                                     19     50       20      30    43     67.6                                     20     50       20      30    47     67.6                                     21     40       20      40    56     69.7                                     ______________________________________                                    

EXAMPLES 22-30

Nine of the fluorine-containing polymers prepared in Examples 10-21 werecured with a bisphenol crosslinking-agent and onium accelerator, and thephysical properties of the resulting cured polymers were determined. 100g of fluorine-containing polymer was mixed with the following curing andcompounding ingredients: 0.862 g of tributyl(2-methoxy)propylphosphonium bisphenoxide AF, which was prepared asdescribed in U.S. Pat. No. 4,882,390 (Grootaert et al.), as a 57.5 wt. %solution in methyl alcohol; 1.23 g of bisphenol AF, as a 70 wt. %solution in ethanol; 30 g of carbon black (Thermax MT™, ASTM N990) asreinforcing agent; 3 g of magnesium oxide (Maglite D™) as acid acceptor;and 6 g calcium hydroxide as acid acceptor.

The compounded polymers were press-cured for 10 min. at 177° C. andpost-cured for 16 hours at 232° C. and physical properties determined.Tensile strength at break, elongation at break, and modulus at 100%elongation were obtained using ASTM Method D 412-80 on a sample cut from1.8 mm sheet of cured polymer with ASTM Die D. Hardness (Shore A) wasmeasured at room temperature on cured samples according to ASTM MethodD-2240-81 using Shore Instrument and Mfg. Co. "A-2" hardness measuringdevice. Compression set was determined using ASTM Method D-395-78 78,Method B, on cured (10 min. press cure at 177° C. followed by 16 hourspostcure at 232° C.) O-rings after 25% compression for 70 hours at 200°C. Compression set is reported as percent of original deformationremaining. The polymers that were compounded and cured, and theresulting physical properties of the cured polymers are summarized inTable 5.

                  TABLE 5                                                         ______________________________________                                             Fluoro-  Tensile  Elonga-                                                                              Modu-       Com-                                Ex.  polymer  strength tion   lus   Hard- pression                            No.  of Ex.*  (MPa)    (%)    (MPa) ness  set (%)                             ______________________________________                                        22   10       11.16    242    4.10  82    27.5                                23   11       9.36     273    3.08  76    34.6                                24   12       14.76    201    6.67  84    29.1                                25   13       11.80    219    4.25  78    27.4                                26   14       14.23    194    6.00  80    24.4                                27   15       10.65    158    5.74  78    26.8                                28   18       7.20     442    2.53  83    47.9                                29   19       15.76    198    7.17  88    28.3                                30   20       15.14    199    6.77  89    27.9                                ______________________________________                                         *compounded and cured as described above                                 

The data in Table 5 show that the polymers of this invention may becompounded and cured to give shaped articles with typicalfluoroelastomer physical-properties.

EXAMPLE 3

In this example, the HFP, VF₂, and TFE tarpolymer of Example 6 was curedas described in Examples 22-30, except that a fluoroaliphaticsulfonamide curing-agent was also used in addition to a bisphenol andonium accelerator.

100 g of the HFP, VF₂, and TFE tarpolymer of Example 6 was mixed withthe following curing agents and compounding ingredients: 0.805 g oftributyl (2-methoxy)propylphosphonium bisphenoxide AF as a 57.5 wt. %solution in methyl alcohol; 1.54 g of bisphenol AF as a 70 wt. %solution in ethanol; 0.5 g N-methyl perfluorooctanesulfonamide, C₈ F₁₇SO₂ NH(CH₃); 30 g of carbon black (Thermax MT™, ASTM N990) asreinforcing agent; 3 g of magnesium oxide (Maglite D™) as acid acceptor;and 6 g calcium hydroxide as acid acceptor.

The compounded fluoroelastomer composition was press-cured andpost-cured, and properties determined as described for Examples 22-30.Physical properties are summarized in Table 6.

                  TABLE 6                                                         ______________________________________                                                Tensile                                                               Ex.     strength Elongation  Modulus                                          No.     (MPa)    (%)         (MPa)  Hardness                                  ______________________________________                                        31      13.59    187         6.12   77                                        ______________________________________                                    

The data in Table 6 show that typical fluoroelastomerphysical-properties were obtained with a polymer of this invention whena fluoroaliphatic sulfonamide was used as a co-curing agent.

EXAMPLE 32

In Example 32, a copolymer of VF₂ and HFP was prepared as in Example 1,except with 4 g (0.023 moles) of octamethyl cyclotetrasiloxane insteadof HMDS, and with 0.6 g FC-128 emulsifier. Reaction time was 5 hrs, with710 g monomer consumed. The polymer was isolated, and analyzed as inExample 1. The Mooney viscosity was 62, and the H-NMR showed thepresence of Si--CH₃ at 0.1 ppm.

Various modifications and alterations of this invention will be apparentto those skilled in the art without departing from the scope and spiritof this invention and this invention should not be restricted to thatset forth herein for illustrative purposes.

What is claimed is:
 1. A fluorine-containing polymer comprising afluorine-containing, saturated, carbon-carbon backbone chain comprisinginterpolymerized units derived from a fluorine-containing ethylenicallyunsaturated monomer, and an organometallic group, derived from anon-free-radically polymerizable organometallic compound, comprising.[.a.]. .Iadd.1 to 10 .Iaddend.silicon .[.atom.]. .Iadd.atoms.Iaddend.and an aliphatic carbon atom bonded directly to .Iadd.one of.Iaddend.said silicon .[.atom.]. .Iadd.atoms.Iaddend..
 2. The polymer ofclaim 1 wherein said backbone chain consists essentially ofinterpolymerized units derived from ethylenically unsaturated monomer.3. The polymer of claim 1 wherein said fluorine-containing monomer isselected from the group consisting of vinylidene fluoride,hexafluoropropene, chlorotrifluoroethylene, 2-chloropentafluoropropene,perfluoroalkyl vinyl ethers, tetrafluoroethylene,1,1-hydropentafluoropropene, 2-hydropentafluoropropene, vinyl fluoride,dichlorodifluoroethylene, perfluorodiallylether, trifluoroethylene, 1,1-dichlorofluoroethylene, and perfluoro-1,3-dioxoles of formula ##STR4##where each R_(f) is F, C_(n) F_(2n+1) where n is from 1 to 4, or wherethe two R_(f) groups together with the carbon atom to which they areattached form a ring of formula C_(n) F_(2n-2) where n is from 5 to 8.4. The polymer of claim 1 wherein .[.said organometallic group comprisesfrom 1 to 200 silicon atoms and wherein .]. said silicon atoms arebonded directly to each other or through an alkylene group, arylenegroup, sulfur atom, oxygen atom, phosphorus atom, nitrogen atom, orcombinations thereof.
 5. The polymer of claim 4 wherein saidorganometallic group is silyl, silazyl, or siloxyl.
 6. The polymer ofclaim 4 wherein said organometallic group has the formula

    R--[(R).sub.2 M].sub.z --[(Q).sub.x --M(R).sub.2 ].sub.y --

M is silicon, Q is a divalent linking group, each R is independently H,alkyl, aryl, or combinations thereof, x is 0 or 1, z is 0 or 1, y is aninteger from 1 to
 9. 7. The polymer of claim 5 wherein saidcarbon-carbon backbone chain consists essentially of interpolymerizedunits derived from one or more monomers selected from the groupconsisting of tetrafluoroethylene, hexafluoropropene, vinylidenefluoride, chlorotrifluoroethylene, ethylene, propylene, perfluoromethylvinyl ether, and perfluoropropylvinyl ether.
 8. The composition of claim6 in its cured state.
 9. A shaped article comprising the polymer ofclaim 1.